Executive Summary

This report for the second quarter, 2001, consists of results from the Environmental Surveillance, Education, and Research (ESER) Program’s monitoring of the Department of Energy’s Idaho National Engineering and Environmental Laboratory’s (INEEL) offsite environment.  All sample types (media) and the sampling schedule followed during 2001 are listed in Appendix A.  This report contains results for the following: 

  • Air sampling, including air filters, charcoal cartridges, and atmospheric moisture,

  • Precipitation,  

  • Drinking and surface water,  

  • Foodstuff sampling, including milk, sheep, large game animals, and marmots, and

  • Environmental radiation.  

Air Sampling

During two weeks, those ending April 11, and May 23, the average gross beta concentration for INEEL locations was significantly higher than at Distant locations.  Also during two weeks, those ending April 18 and May 23, the average gross beta concentration for INEEL locations was significantly higher than at Boundary locations.  During one week (April 11), the average gross beta concentration was higher at Boundary locations than at Distant locations. 

The average gross alpha concentration for INEEL locations was significantly higher than at Distant locations during two weeks, those ending April 4, and June 20.  During those same weeks, the average gross alpha concentration at Boundary locations was significantly higher than Distant locations.  There were no consistent trends (for either gross alpha or gross beta) over time where INEEL was higher than Boundary, which was higher than Distant locations as one would expect if the INEEL was the source of radionuclide contamination.   Gross alpha and gross beta results for individual filters are listed in Table C-1 of Appendix C. 

Monthly average gross alpha and beta concentrations in air at each sampling location are shown in Figures 10 – 15.  No 131I was detected in any of the weekly charcoal cartridges during the second quarter.   Weekly 131I results for each location are listed in Table C-2 of Appendix C.

Weekly filters for the second quarter of 2001 were composited by location.  Selected locations were analyzed for the gamma emitting radionuclides, 90Sr, 238Pu, 239/240Pu, and 241Am.  No 238Pu or 137Cs were detected on any of the composite samples.  Of the nine samples submitted for analysis, 241Am was detected in five of them.  Four of the five samples had levels greater than their respective 2s and minimum detectable concentrations (MDC) (see Table 2).  One sample, from the Arco QA-1 station, had an 241Am result greater than 2s, but less than the MDC.  239/240Pu was detected in four of the samples submitted.  Three of the four samples had levels greater than their respective 2s and MDCs (see Table 2).  One sample, from the Main Gate location, had a result greater than 2s, but less than the MDC.  90Sr was detected in two of the samples submitted at a level greater than their associated 2s values, but less than the MDCs, indicating they are most likely false positives.  Concentrations were within the range of values measured throughout the World.  In addition, detected values in composite samples for 241Am ranged from 5,100 to over 10,500 times smaller than the derived concentration guide (DCG) value.  Values detected in composite samples for 239/240Pu ranged from 5,800 to over 17,500 times smaller than the DCG value.  Details of both weekly and quarterly analyses can be found in section 3.1. 

Nine atmospheric moisture samples were obtained during the second quarter of 2001 - three from Rexburg CMS, three from Blackfoot CMS, two from Atomic City and one from Idaho Falls.  Five samples were greater than their associated 2s uncertainty and MDC (Table 3).  For comparison, the results measured at these locations during the second quarter of 2001 were between 87,000 and 225,000 times lower than the DCG value for tritium in air (as atmospheric moisture) of 1 x 10-7 µCi/mL (3.7 x 10-3 Bq/mL) (see Table B-1).  Tritium results for all atmospheric moisture samples are listed in Table C-4 (Appendix C).

PM10 concentrations for the second quarter of 2001 were well below all air quality standard levels.  The maximum 24-hour concentration was 44.9 µg/m3 on April 18, at Rexburg CMS.  Results for all PM10 samples are listed in Table C-5, Appendix C. 

For the second quarter of 2001, there was enough precipitation for a total of six samples – two monthly composites from Idaho Falls, two monthly composites from the Central Facilities Area (CFA), and two weekly samples from the Experimental Field Station (EFS).  Of the precipitation samples collected, two EFS samples (collected on April 4 and April 18) yielded tritium results greater than the 2s uncertainty.  The sample collected on April 4 did not exceed the MDC, while the sample collected on April 18 did exceed the MDC (see MDC values).  Tritium was also detected above the 2s level in the Idaho Falls sample in May and the duplicate sample from Idaho Falls in June.  However, neither of these samples exceeded their associated MDC, indicating false positives.   While there are no specific limits on the amount of tritium in precipitation, as a comparison the Safe Drinking Water Act (SDWA) limits tritium in drinking water to 2 x 104 pCi/L (Appendix B-1).  The level of tritium detected in the sample from EFS that was above its associated 2s and MDC value was 140 times lower than the SDWA limit.

Water Sampling

Fourteen drinking water samples were collected from selected taps throughout southeast Idaho (Figure 16).  Samples were analyzed for gross alpha, gross beta, and tritium (3H).  Only the water samples from Fort Hall and Moreland were above 2s and above the MDC for tritium.  All drinking water samples had gross beta results above 2s, and all but four (those from Carey, Arco, Howe and Idaho Falls) were greater than their associated MDCs.  Of the samples analyzed for gross alpha, four, those from Minidoka, Arco, Atomic City, and Monteview, were greater than 2s and their associated MDCs.  

The level of tritium detected in the samples from Fort Hall and Moreland that were above 2s and the MDC were 155 to 179 times lower than the SDWA limit.  The measured levels were also within the range of background tritium that exists throughout the world.  The level of gross beta detected in the samples that were above 2s and the MDC were between 4 to 18 times lower than the SDWA limit.  The level of gross beta detected in the samples that were above 2s and the MDC were between 7 to 20 times lower than the SDWA limit.  Levels of gross alpha and gross beta observed are not unusual given the basaltic terrain (USGS 1991).  All values are similar to those recorded in previous years, and are well below the levels outlined for drinking water. 

Five surface water samples and one duplicate sample were collected from locations throughout southeast Idaho and analyzed for tritium, gross alpha, and gross beta.  Results for tritium analyses showed that only one sample (Idaho Falls) was above its 2s and MDC.  At the reported level, the tritium result is 83 times smaller than the SDWA limit, and 333 times smaller than the DCG value.  Analytical results for gross alpha showed that the samples from Bliss and Buhl exceeded their 2s and MDC values (Table 6).  At reported levels, the gross alpha values are between 13.6 and 16.5 times lower than the SDWA limit and between 27.3 to 33.0 times lower than the DCG value.  Results for gross beta for all five surface water samples, and the duplicate from Buhl, were greater than their associated 2s and MDC values (Table 6).  The gross beta values are between 7.7 and 16.8 times lower than the SDWA levels, and between 15.4 to 33.6 times lower than DCG values.

Food Sampling 

Milk samples were collected weekly in Idaho Falls and monthly at nine other locations around the INEEL (Figure 17), and analyzed for gamma emitting radionuclides.  No samples had a 137Cs concentration greater than the 2s uncertainty.  One sample from Rupert (dated April 3) had an 131I result greater than the 2s and MDC, however, an immediate recount showed the sample did not exceed either the 2s or MDC, thus indicating a false positive.  Of the six samples submitted for 90Sr analysis, all of them had concentrations of 90Sr greater than the 2s level, and three were above their associated MDC (Carey, Rupert, Blackfoot).  Of the four samples submitted for tritium analysis only one had a concentration greater than its associated 2s (Roberts). 

While there are no specific regulatory limits for 90Sr in milk, as a comparison, the DCG for 90Sr of 1.0 x 10-6 µCi/ml in water can be used.  Samples that exceeded both the 2s and MDC were from 1,209 to 1,330 times smaller than the DCG value.  Further information on second quarter milk samples can be found in section 5.1.

Individual sheep from three separate flocks were sampled including a control flock in Dubois from the Experimental Sheep Station, a flock from a southern INEEL allotment, and a flock from a northern INEEL allotment.  Two sheep were taken from each flock.  Thyroid, muscle, and liver tissue were collected and analyzed for gamma emitting radionuclides.  No 131I was found in any of the samples.  Analysis for 137Cs showed results greater than 2s in three samples from two separate sheep:  one muscle and one liver sample collected from the same lamb on the Northern allotment on May 18, and one muscle sample collected May 9, from a lamb on the Southern allotment.  All concentrations of 137Cs were similar to those found in both onsite and offsite sheep samples during recent years.

Environmental Dosimeters

Environmental dosimeter locations are divided into Boundary and Distant groupings.  Boundary exposure rates ranged from 0.33 to 0.37 mR/day.  The overall average was 0.35 mR/day.  The Distant set ranged from 0.32 to 0.41 mR/day.  The average Distant value was 0.36 mR/day.  No statistical difference existed between Boundary and Distant locations.  Furthermore, all values are in line with past readings.  Table 5 lists the range and average for both groups. 

Summary

All concentrations of radioactivity found in samples collected by the ESER program during the second quarter, 2001 were consistent with concentrations that have been found in samples taken during recent years.   The ESER program could not directly attribute measured concentrations to operations at the INEEL.  Radionuclide concentrations in all of the samples collected and analyzed were below guidelines set by both the DOE and the Environmental Protection Agency (EPA) for protection of human health.

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